| Type | Description |
|---|---|
| Definition | intraflagellar transport 172 |
| Date | Results | Publications |
|---|---|---|
| 2019-02-16 12:14:00 | This mouse model exhibits key features of the retinal phenotype observed in patients with IFT172-associated blindness and can be used for in vivo testing of ciliopathy therapies. | 29659833 |
| 2012-01-21 10:10:00 | Mutation of Ift172 results in a specific class of abnormal cilia and resulting in the VACTERL-like features with hydrocephalus phenotype. | 21653639 |
| 2010-04-12 12:01:00 | Phenotype of the disrupted allele by using CRE expression directed by the prx1 enhancer to disrupt the conditional Ift172 allele in the developing limb. | 19521792 |
| 2010-01-21 00:00:00 | The formation and function of the node and anterior mesendoderm in the mouse embryo relies on an indispensable role of Ift172 in cilia morphogenesis and cilia-mediated signaling. | 18930042 |
| 2010-01-21 00:00:00 | identification of two mouse mutants, wimple (wim) and flexo (fxo), that lack ventral neural cell types and show other phenotypes characteristic of defects in Sonic hedgehog signalling | 14603322 |
| Type | IDs |
|---|---|
| Synonymous | 4930553F24Rik, Slb, avc1, wim |
| Gene |
UniProtKB-ID:
IF172_MOUSE
UniprotKB:
Q6VH22
UniParc:
UPI00000253D3,
UPI000021C0F9
EMBL:
BC066096,
AK006007,
AY339616,
BC051928,
BC060948,
AK122461
Ensembl:
ENSMUSG00000038564
KO:
mmu:67661
|
| Nucleutide sequences |
EMBL-CDS:
AAH51928.1,
AAH66096.1,
AAR05390.1,
BAB24362.1,
BAC65743.3,
AAH60948.1
Ensembl_TRS:
ENSMUST00000041565
|
| Protein sequencees |
Ensembl_PRO:
ENSMUSP00000049335
RefSeq:
NP_080574.5
|
| Others |
UniRef100:
UniRef100_Q6VH22
UniRef90:
UniRef90_Q6VH22
UniRef50:
UniRef50_Q6VH22
UniGene:
Mm.293023
CCDS:
CCDS39054.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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